Zhang Qiang, Colazo Juan, Berg Darren, Mugo Samuel M, Serpe Michael J
Department of Chemistry, University of Alberta , Edmonton, Alberta T6G 2G2, Canada.
Physical Sciences Department, MacEwan University , Edmonton, AB T5J 4S2, Canada.
Mol Pharm. 2017 Aug 7;14(8):2624-2628. doi: 10.1021/acs.molpharmaceut.7b00325. Epub 2017 Jul 7.
Nanogels with a biomolecular coating (biocoating) were shown to be capable of triggered delivery of anticancer drug Doxorubicin. The biocoating was formed utilizing binding between glycogen and the tetra-functional lectin Concanavalin A, which can be triggered to disassemble (and release) upon exposure to glucose and changes in solution pH. We also show the nanogel's thermoresponsivity can be used to accelerate Doxorubicin release. Moreover, we showed that transferrin immobilized on the nanogel surface could accelerate nanogel uptake by cancer cells. In these experiments, we showed that Doxorubicin was able to be released to the nucleus of human liver cancer cell line (HepG2) within 3 h. Doxorubicin-loaded nanogels exhibit a strong growth inhibition ability toward HepG2. This investigation showcases how nanogel design and chemistry can be tuned to achieve useful biomedical applications.
具有生物分子涂层(生物涂层)的纳米凝胶已被证明能够触发抗癌药物阿霉素的递送。生物涂层是利用糖原与四功能凝集素伴刀豆球蛋白A之间的结合形成的,当暴露于葡萄糖和溶液pH值变化时,这种结合可被触发分解(并释放)。我们还表明,纳米凝胶的热响应性可用于加速阿霉素的释放。此外,我们发现固定在纳米凝胶表面的转铁蛋白可以加速癌细胞对纳米凝胶的摄取。在这些实验中,我们表明阿霉素能够在3小时内释放到人类肝癌细胞系(HepG2)的细胞核中。负载阿霉素的纳米凝胶对HepG2表现出很强的生长抑制能力。这项研究展示了如何调整纳米凝胶的设计和化学性质以实现有用的生物医学应用。